| Poster Number | Proposal Name | First Name | Last name |
| Day 1 | |||
| ASD 1 | Streamlining the genetics pipeline to increase testing for patients at risk for hereditary prostate cancer: the UCSF Prostate Cancer Genetic Testing Station. | Fern | Alagala |
| ASD 2 | COVID workflow adjustments impact where, when, and how genetic counseling was delivered early in the pandemic | Cary | Armstrong |
| ASD 3 | Family History Collection, Genetic Risk Assessment, and Use of Digital Health Tools by Obstetricians | Hitashi | Bansal |
| ASD 4 | Utilization of Genetics Services in the Diagnosis of Hearing Loss in Newborns in the State of Ohio | Cara | Barnett |
| ASD 5 | Genomic Testing in Healthy Individuals: The Brigham Preventive Genomics Clinic | Tala | Berro |
| ASD 6 | "It's the same as if you did meet them in person" The Genetic Patient's Perspective on Telehealth Consultations | Emily | Bonnell |
| ASD 7 | One Cancer Genetic Counseling Clinic’s Response to COVID-19: ‘Ghost Protocol’ | Christine | Bruha Steele |
| ASD 8 | Evaluation of Family Group Telehealth Genetic Counseling Services | Natasha | Chadburn |
| ASD 9 | Genetic counseling in the inpatient care setting: genetic counselors perceive that on-demand services are valuable to patients and providers | Cheyla | Clark |
| ASD 10 | Integration of universal genetic counseling and testing for newly diagnosed breast cancer patients | Julie O. | Culver |
| ASD 11 | Genetic Counselor Perceptions of Patient Outcomes from Non-Genetics Providers Offering Genetic Services | Katharine | Drum |
| ASD 12 | Implementation and Evaluation of a Genetic Services Referral Phone Line in the New York-Mid-Atlantic Consortium (NYMAC) Region | Alyson E. | Evans, MS |
| ASD 13 | How Much We Tell Our Patients: Counseling Differences between Genetic Counselors and Other Providers | Jessica | Feldman |
| ASD 14 | Patient satisfaction with direct telegenetic counseling for prenatal compared to hereditary cancer indications | Kristi | Fissell |
| ASD 15 | Perceptions of Genetic Counseling and Testing in the Haitian Patient Population | Elizabeth | Francisco |
| ASD 16 | Delivering Bad News in Genetic Counseling via Telephone: Evaluating Distress, Perceived Personal Control, and Satisfaction in Patients | Allison | Gossen |
| ASD 17 | “You’re in charge of your health”: Perspectives of hereditary cancer population screening participants | Veronica | Greve |
| ASD 18 | Comparing Clinician-Parent Communication Patterns During Genome Sequencing Result Disclosures in a NICU Setting | Brittany | Griffin |
| ASD 19 | Satisfaction with online pre-test education, at-home BRCA screening, and telehealth genetic counseling in the Ashkenazi Jewish population: an Atlanta pilot study | Melanie W. | Hardy, MS, MS, CGC |
| ASD 20 | Assessment of Understanding and Satisfaction of Clinical Exome Sequencing (ES): Video Consent vs Telephone Consent | Hannah | Helber |
| ASD 21 | A Novel Genetic Testing Reminder System Using an Online Signature Platform | Sayoni | Lahiri |
| ASD 22 | Extending the Reach of Cancer Genetic Counseling to the Safety Net: Effectiveness of Genetic Counseling across Three Modes of Delivery | Robin | Lee |
| ASD 23 | Characterization of Genetic Counselor Practices in Inpatient Care Settings | Emily | Magness |
| ASD 24 | The Innovative Use of RedCap as a Means to Recontact Patients with Hereditary Cancer | Caitlin | Mauer |
| ASD 25 | Telegenetics vs. In-Person Satellite Clinic- Patient acceptance and effect on access and adherence | Ryan | Noss |
| ASD 26 | Exploring South Asian Perspectives on Genetic Counseling | Shabri | Patel |
| ASD 27 | SHAPING A DIALOGUE: INSIGHTS FROM THE SICKLE CELL COMMUNITY ON GENETICS HEALTHCARE | Diana | Phan |
| ASD 28 | Patient satisfaction with Genetic Results Counseling service | Ellen | Schlenker |
| ASD 29 | Characterization of genetic counseling follow-up decisions among patients with a medically actionable result from genomic screening | Marci | Schwartz |
| ASD 30 | Exploring perceptions and attitudes towards integrating a genetic counselor into a multidisciplinary primary care practice team. A qualitative GenCOUNSEL study | Caitlin | Slomp |
| ASD 31 | Genetic counselors leveraging technology: Integrating telemedicine into general genetics clinic via pre-clinic screening | Christine | Spaeth |
| ASD 32 | Inherited Retinal Degeneration Current Genetics Practices – A Needs Assessment | Sydney | Strait |
| ASD 33 | Custom automated software tools increase genetic counseling follow-up task efficiency | Kelly | Tangney |
| ASD 34 | Adapting Genetic Testing Results Disclosures to Patient Preferences at the Prostate Cancer Genetic Testing Station | Barry | Tong |
| ASD 35 | Should All Patients with Breast Cancer be Offered Genetic Testing? Reactions to the ASBrS Consensus Guideline on Genetic Testing for Hereditary Breast Cancer | Kelly | Tripi |
| ASD 36 | Impact of a GCA on genetic counselor efficiency in a cancer genetics clinic | Meghan | Vanwanzeele |
| ASD 37 | How Do Genetic Counselors and Genetic Counseling Assistants Spend Their Time? A Workflow Analysis | Siddika | Venkatachalam |
| ASD 38 | Barriers Remaining After the Integration of Genetic Counseling in a Multi-Disciplinary Pancreatic Cancer Clinic | Elise | Watson |
| ASD 39 | A Snapshot of Consumer-Initiated Genetic Testing: A Demographic Chart Review | Nori | Williams |
| ASD 40 | Motivations For Ordering Consumer-Initiated Genetic Testing: A Chart Review | Nori | Williams, CGC |
| ASD 41 | Refining a Tool to Automate Portions of Pre-Test Genetic Counseling for Inherited Cancer | Brenda | Zuniga |
| ADT 42 | Familial Partial Lipodystrophy Type 2 and 3 due to Likely Pathogenic LMNA and PPARG Variants Identified in Two Individuals with Atypical Presentations | Colby | Chase |
| ADT 43 | DTC Ancestry Testing Reveals a 46,XX Male and Infertility | Kelly | East |
| ADT 44 | Identification of a pathogenic MECP2 variant in two adults presenting to a Medical Genetics clinic with intellectual disability | Anna | Raper, MS, CGC |
| ADT 45 | The Perspective of Men with Barth Syndrome: Relationship Building, Family Planning, and Reproductive Decision-Making | Jason | Shandler |
| ADT 46 | eMERGE Consortium Participant Reported Sharing of Genomic Screening Results with Family Members. | Julia | Wynn |
| CAN 47 | CTNNA1 Reclassified From Pathogenic To a Variant of Unknown Significance In a Breast Cancer Patient: Managing Patient and Counselor Expectations | Dina | Alaeddin |
| CAN 48 | Somatic Tumor Testing Implications for Lynch Syndrome Germline Genetic Testing | Kathleen | Barrus |
| CAN 49 | Breast cancer in PMS2-positive patients | Kylin | Boehler |
| CAN 50 | Positive Patient BRCA1/2 Direct-to-Consumer Genetic Testing Results: Now What? | Sarah | Burke |
| CAN 51 | Case of BRCA Double Heterozygosity in a Non-Ashkenazi Jewish Individual | Cara | Cacioppo |
| CAN 52 | Utilization of broad approaches of genetic counseling and testing to better understand pediatric cancer predisposition | Katie | Church |
| CAN 53 | Risk Reducing Mastectomies among Women with Mutations in Moderate Penetrance Breast Cancer Susceptibility Genes | Jacob | Comeaux |
| CAN 54 | Reported Phenotype in Individuals with NF1 Pathogenic Variants Identified by Panel Testing | Lauren | Currie |
| CAN 55 | Trends in Ordering Patterns of Hereditary Cancer Panels | Lauren | Currie |
| CAN 56 | A novel case of lobular breast cancer in a male patient with a pathogenic mutation in CDH1 | Matthew | Emery |
| CAN 57 | Co-occurrence of attenuated familial adenomatous polyposis (AFAP) and Lynch syndrome: A case report with implications for surveillance. | Jamie | Fisher |
| CAN 58 | Genetic counselors’ use of multi-gene panels in cancer genetics: A quantitative study | Natasha | Fuller |
| CAN 59 | Expanding Phenotypes for Male BARD1 Carriers: A Case Report | Melissa | Gandhi |
| CAN 60 | Discrepant CDKN2A c.146T>C variant: a clinical experience | Amber | Gemmell |
| CAN 61 | Motivations for Pursuing Genetic Counseling to Explore the Availability of Panel Genetic Testing | Jessalyn | Gerber |
| CAN 62 | Toward a Better Understanding of the Experience of Patients with Moderate Penetrance Breast Cancer Gene Mutations: A focus on ATM and CHEK2 | Carly | Grant |
| CAN 63 | Who would have been missed? A comparison of current and past hereditary cancer testing guidelines in a large prospective universal testing study | Megan | Hager |
| CAN 64 | Pathogenic variant classifications are not always well-supported by evidence | Sarah M. | Hamilton |
| CAN 65 | An Extended Case Series of Gastrointestinal Neoplasms in Li-Fraumeni Syndrome | Jessica | Hatton |
| CAN 66 | Families with Rare POT1 Variants Identified Through Multigene Panel Testing | Marie-Louise | Henry |
| CAN 67 | Implementation of Hereditary Genetic Testing for All Patients with a Personal History of Breast Cancer: Perspectives of Key Healthcare Professionals | Kyle | Heraty |
| CAN 68 | Melanoma Risk in POT1 Mutation Carriers from a MGPT Cohort | Jennifer | Herrera-mullar |
| CAN 69 | Site-Specific Analysis vs. Multi-Gene Panel Testing for Familial Cancer Variants: Current Practices of Genetic Counselors | Eleanor | Hilton |
| CAN 70 | Review Process of Somatic Tumor Reports for Genetic Counseling Referrals | Brenda | Ho |
| CAN 71 | De novo TP53 variant in a child with early onset rhabdomyosarcoma and maternal history of gestational choriocarcinoma | Sarah E | Jennings |
| CAN 72 | Attitudes and Practices of Genetic Counselors towards Hereditary Cancer Syndromes with Associations of Unclear or Conflicting Evidence | Kerry | Johnson |
| CAN 73 | Evaluation of Pilot Program to Implement Breast Cancer Risk Assessment at Screening Mammography in One US Health System | Alanna | Kulchak Rahm |
| CAN 74 | Expanding the detection range of DNA multigene panel testing with concurrent RNA sequencing | Holly | LaDuca |
| CAN 75 | An Interpretative Phenomenological Analysis: The Lived Experience of Emerging Adults at Risk for Gastric Cancer Due to a CDH1 Variant in Medical Management Decision Making | Yi | Liu |
| CAN 76 | Real-world Multi-Country Study of Germline BRCA1/2 Mutation (gBRCA1/2mut) Testing and Genetic Counseling (GC) Among Patients (pts) With Human Epidermal Growth Factor Receptor 2-Negative (HER2-) Advanced Breast Cancer (ABC) | Reshma | Mahtani |
| CAN 77 | Inconclusive genetic test results and a phenotype possibly confounded by prior childhood cancer | Rachelle | Manookian |
| CAN 78 | Double heterozygosity for RET and PTEN: one family’s phenotype | Nicole | Mans |
| CAN 79 | A case report of an incidental germline AXIN2 likely pathogenic variant in a patient with ovarian cancer | Kimberly | Matthijssen |
| CAN 80 | Development and Initial Outcomes of a Hereditary Hematologic Malignancies Clinic | Kelsey | Moriarty |
| CAN 81 | A case of an infant with Beckwith Wiedemann syndrome and Marfan syndrome: The value of taking a family history | Alise | Murray |
| CAN 82 | An unexpected diagnosis of MUTYH-associated polyposis: A case study | Honey | Nagakura |
| CAN 83 | Comprehensive germline multigene panels change clinical care and inform treatment strategies for breast cancer patients | Sarah M | Nielsen |
| CAN 84 | Genetic Counselors’ Attitudes and Practices Regarding Preimplantation Genetic Testing for Hereditary Breast and Ovarian Cancer | Hannah | Novak |
| CAN 85 | Sources of Community Referrals to a Pediatric Cancer Predisposition Clinic: Opportunities for Outreach | Regina | Nuccio, MS, CGC |
| CAN 86 | IMPLEMENTING BRCA MAINSTREAMING IN AUSTRALIA: A QUALITATIVE STUDY | Rosie | O Shea |
| CAN 87 | Genetic Counseling (GC) Patterns by Practice Setting Among Patients (pts) With Germline BRCA1/2 Mutated (gBRCA1/2mut) Advanced Breast Cancer (ABC): Results From a US Retrospective Medical Records Review Study | Elias | Obeid |
| CAN 88 | A Process Improvement Analysis of Referral Rates to Genetic Counseling for Consideration of Germline Genetic Testing After Receipt of Somatic Genetic Testing Results | Rachel | Paul |
| CAN 89 | BRIP1: An institutional experience with a dynamic gene | Sara | Pirzadeh-Miller |
| CAN 90 | “I wish that there was more info”: Characterizing the uncertainty experienced by carriers of pathogenic ATM and/or CHEK2 variants | Kathryn | Reyes |
| CAN 91 | Exploring Current Practices and Perspectives of Genetic Counselors on DNA Biobanking in Oncology | Hillary | Rieger |
| CAN 92 | A Qualitative Study of Transgender Patients’ Perspectives on their Cancer Genetic Counseling Experiences | Lathel | Rolle |
| CAN 93 | Impact of Genetic Based Melanoma Risk Assessment on Attitudes and Preventative Behaviors | Kaylee | Ruiz |
| CAN 94 | An Analysis of the Lived Experience of Patients Incidentally Found to Carry a Pathogenic TP53 Mutation | Emily | Seckington |
| CAN 95 | Rapid Adaptation and Evaluation of a Telemedicine-Only Cancer Genetic Counseling Model in the COVID-19 Pandemic | Margaret | Sheehan |
| CAN 96 | A Postmortem End to the Diagnostic Odyssey: The Diagnosis of Noonan Syndrome in a Boy with ALL and Secondary T-Lymphoblastic Lymphoma | Susan | Shehayeb |
| CAN 97 | Psychosocial Outcomes Following An Abnormal ctDNA-Based Cancer Screening Test | Gabrielle T. | Shermanski, MS |
| CAN 98 | Provider Experiences with Incidental Germline Findings Revealed Through Somatic Sequencing in Oncology | Ilana | Solomon |
| CAN 99 | The Impact of the “American Society of Breast Surgeon’s 2019 Consensus Guidelines on Genetic Testing for Hereditary Breast Cancer” on Cancer Genetic Counselors | Jillian | Tokarczyk |
| CAN 100 | Germline pathogenic/likely pathogenic variant incidence in individuals with colorectal cancer stratified by age at diagnosis | Natalie | Tri |
| CAN 101 | Atypical genetic causes of Lynch syndrome: a case series | Magan | Trottier |
| CAN 102 | Frequency of 5 Cancer Types in Families with a Pathogenic or Likely Pathogenic Variant in the ATM Gene | Diana Moglia | Tully |
| CAN 103 | Mosaic STK11 Mutation in the Context of a Clinical Diagnosis of Peutz-Jeghers Syndrome (PJS) and Ashkenazi Jewish Ancestry: Genetic Counseling Opportunities and Challenges | Morgan | Turner, MS, CGC |
| CAN 104 | Clinical Presentation of Individuals with Pathogenic/Likely Pathogenic TP53 Variants Detected via Different Ascertainment Methods: a Case Series | Julia | Weston |
| CAN 105 | Factors in Screen Adherence Across the Lifespan in Individuals with Rare Hereditary Cancer Syndromes | Amy | Whitburn |
| CAN 106 | The Phenotype of POT1 Pathogenic Variant Carriers | Elizabeth | Wiley |
| CAN 107 | Early-onset triple negative breast cancer for a family with a likely pathogenic RAD51C mutation: considerations for improved screening and surveillance | Edward | Williams |
| CAN 108 | From Business Plan to a Three-Year Implementation Review: Successes/Challenges for the solo genetic counseling establishing hereditary cancer risk assessment and risk education | Edward | Williams |
| CAN 109 | A pilot study of breast cancer polygenic risk scores shows discrepancies between laboratories. | Julia | Wynn |
| CAN 110 | Neuroblastoma and Cutaneous Angiosarcoma in a Child with PTEN Hamartoma Tumor Syndrome | Kristin | Zelley |
| CAN 111 | Evaluation of Genetic Counseling Referral Rates Before and After Inclusion of Genetic Counselor Attendance at Gynecologic Oncology Tumor Board | Marie | Zerjav |
| CAR 113 | What Makes at-risk Family Members Pursue Cascade Genetic Testing for Hypertrophic Cardiomyopathy? | Emily | Callahan |
| CAR 114 | Development of Death Investigator Education on Genetics and Postmortem Genetic Testing - A Pilot Study | Rachel | Campagna |
| CAR 115 | Risk perception and screening behaviors in individuals with an inherited predisposition for Hypertrophic Cardiomyopathy | Melanie | Emmerson |
| CAR 116 | Exploring the Communication of Cardiac-Related Risk to First-Degree Relatives After the Sudden Death of a Young Family Member | Martha | Francoeur |
| CAR 117 | Genetic counseling for bicuspid aortic valve: Predictors of knowledge, empowerment, and familial uptake of cardiac screening | Bailey | Hancock |
| CAR 118 | Comprehensive Analysis of Cardiomyopathy and Arrhythmia Genes Yields Unanticipated Molecular Diagnoses | Ana | Morales |
| CAR 119 | Exploring Lab vs. Clinical Discrepancies in Five Genes Known to Cause Loeys-Dietz Syndrome | Mitchel | Pariani |
| CAR 120 | Investigating Medical Examiners’ Practices: Genetic Evaluation for Fatal Acute Aortic Dissection | Bradley | Power |
| CAR 121 | Pediatric Primary Care Providers Use of And Adherence to Cholesterol Screening Guidelines When Assessing Patients For Hypercholesterolemia: A Qualitative Assessment of Providers In Minnesota And California | Jenna | Soukup |
| CAR 122 | Applying Motivational Interviewing Strategies with the Extended Parallel Process Model to Improve Risk Communication for Parents of Children with Familial Hypercholesterolemia | Bridget | Winchester |
| CAR 123 | Outcomes from a Novel Genetic Counseling Intervention Using Motivational Interviewing and The Extended Parallel Process Model to Increase Cascade Cholesterol Screening | Heather | Zierhut |
| CPI 124 | Exploration of Patient Attitudes toward Receiving Incidental Diagnoses of Lysosomal Storage Disorders Through Expanded Carrier Screening | Allison | Abbott |
| CPI 125 | Getting punched in the gut – The experience of families receiving a negative genome-wide sequencing result | Shelin | Adam, MSc |
| CPI 126 | The Impact of Hindu Philosophy on Perspectives of Hindu Women on Pregnancy Termination | Amanda | Back |
| CPI 127 | Depression Screening Practices of Prenatal Genetic Counselors | Sarah | Belsky |
| CPI 128 | Time well spent: Lessons learned from a qualitative study exploring parental reactions to genetic counseling patient letters after a pediatric visit | Courtney | Brown |
| CPI 129 | Decision-Making in Mental Health Referral: The Influence of Genetic Counselor Emotion | Hannah | Campbell |
| CPI 130 | Discordant Interpretations of Germline Variants in Hereditary Cancer - A Psychosocial Burden? | Meera | Clytone |
| CPI 131 | Simpatía y Respeto: Spanish speaking genetic counselors’ perceptions of language concordance in genetic counseling sessions | Amanda | de Leon |
| CPI 132 | Proxy Patient's Perceptions of Genetic Counselor's Empathy Responses | Jennine | Deckert |
| CPI 133 | Calculating and Communicating Error Estimates For Pathogenic Variant Classifications | Julie M. | Eggington |
| CPI 134 | An Exploration of the Psychosocial Impact of Gene Therapy for Individuals with Hemophilia | Haley | Fischman |
| CPI 135 | Experiences and Perspectives of Patients who Have Considered or Undergone Transfer of Embryos with Mosaic PGT-A Results | Eva | Gabor-Fourcade |
| CPI 136 | Genetic counselors' practices and perceptions when counseling native clients | Hannah | Garn |
| CPI 137 | Investigating factors that influence genetic counselors’ decisions to refer patients to mental health providers | Taylor | Hayes |
| CPI 138 | Use of NCCN Distress Thermometer in Cancer Genetics Patients | Michelle F. | Jacobs |
| CPI 139 | Hispanic Patients’ Perspectives on Language-Concordant Cancer Genetic Counseling Sessions | Sharisse | Jimenez |
| CPI 140 | Characterizing the Mental Health Referral Process in Genetic Counseling | Colleen | Jodarski |
| CPI 141 | Are genetic counselors prepared to counsel active-duty service members? | Michael | Kamen |
| CPI 142 | Review of patients who actively decline recommended CIT post-test genetic counseling | Robin | King |
| CPI 143 | Psychological Distress in Response to Physical Activity Restrictions in Patients with Non-syndromic Thoracic Aortic Aneurysm/Dissection | Alexis | McEntire |
| CPI 144 | Exploring the impact of empathy-based practice on a genetic counselor’s emotional state during their pregnancy | Emma | Moores |
| CPI 145 | From bookbags to company cars: A window into the experiences of growing up with an undiagnosed medical condition | Christina | Pool |
| CPI 146 | The Psychosocial Impact of Having a Child with Usher Syndrome: What Can be Done to Better Meet the Needs of Parents and Caregivers | Rachel | Rabenn |
| CPI 147 | Issues of countertransference in providing reproductive genetic counseling for a patient with SMA type II | Jill | Slamon |
| CPI 148 | Genetic Testing and Counseling for Asian Americans: A Systematic Review | Jennifer | Young |
| EDU 149 | Graduate Training Experiences of Genetic Counseling Students in the United States and Canada | Pauline | Aamodt |
| EDU 150 | Genetic Counseling Graduate Programs: Is a Standardized Application Possible? | Erin | Beasley, BA |
| EDU 151 | Bayes for Days: Development of a Case-Based Risk Assessment Course for Genetic Counselors | Grace | Bronken, MS |
| EDU 152 | Genetics Knowledge of Patients with Hereditary TTR Amyloidosis | Emily | Brown |
| EDU 153 | Group Meditation, Addressing Stigma, and ‘Mental Health Days’: Recommendations for Integrating Self-Awareness Practices into Genetic Counseling Graduate Programs | Laura | Bulmer, MS |
| EDU 154 | Impact of Medical Improv Training on Preparation Genetic Counseling Assistants for Graduate School Interviews | Remington | Fenter |
| EDU 155 | Exploring the Impact of a Variant Curation Module in the Undergraduate Classroom | Kassandra | Grimm |
| EDU 156 | Creating and Evaluating a Tool to Support Families Receiving Genomic Testing Results | Julia | Handra |
| EDU 157 | Two Cycles In: Investigating Admissions Committee Members’ Perspective on the Genetic Counseling Match | Eileen | Hoffman |
| EDU 158 | Genetic Counseling Assistant-Run Clinic: Enhancing Prospective Genetic Counselors’ Skill Sets and Improving Clinic Efficiencies | Caitlin | Mauer |
| EDU 159 | Digital peer-to-peer sharing: Online opportunities for NBS education | Brianne | Miller |
| EDU 160 | Podcast Development to Train Genetic Counseling Clinical Supervisors: A Pilot Study | Rebecca | Padersky |
| EDU 161 | Exploring Genetic Counseling Students' Experiences with the Job Search and the Impact of Clinical Training | Haewon | Park |
| EDU 162 | Development of a Graduate Certificate in Genomics for Genetic Counselors at UBC | Anastasia | Richardson |
| EDU 163 | Assessing the training of current genetic counseling students related to pharmacogenomic testing | Daniel | Serber |
| EDU 164 | Are Genetic Counseling Graduates Prepared to Counsel on Health Insurance Coverage and Costs of Genetic Testing? | Hannah | Sigurdson |
| EDU 165 | Anger, Fear, and Sadness: Differences in Genetic Counseling Student Responses to Intense Patient Affect | Rachel | Simon |
| EDU 166 | Assessing the Current State of Affairs Surrounding Education on Counseling Direct-to-Consumer Testing Patients Through Surveying Genetic Counseling Program Directors | Erin | Swartz |
| EDU 167 | Pharmacogenetics and Direct-to-Consumer Testing: A Knowledge Gap in the Genetic Counseling Community | Alora | Terry, MS, GC |
| EDU 168 | The Development of a Telehealth Rotation in Response to Program Needs | Shannon | Wieloch |
| EDU 169 | Genetic Counseling Student Remote Rotation in ClinGen Variant Interpretation: Expanding Training Options | Diane | Zastrow |
| ELS 170 | Defining the Critical Components of Informed Consent for Genetic Testing | Maia | Borensztein |
| ELS 171 | Increasing recruitment of patients with undiagnosed diseases from underserved populations in the Pacific Northwest | Brenna | Boyd |
| ELS 172 | Impact of Psychiatric Genetic Data on Tort Litigation and its Relationship with Stigma | Kira | Dineen, MS, GC, CG(ASCP)CM |
| ELS 173 | Understanding genetic counselors' perceptions of a duty to warn | Alexis | Lash |
| ELS 174 | Impact of ancestry-related test limitations on informed consent and pre-test genetic counseling | Joseph | Liu |
| ELS 175 | Ethical Considerations for X-ALD Screen-Positive Females on State Newborn Screening | Claire | Newman, MS, CGC |
| ELS 176 | The Role of GenomeConnect in Keeping Patients Updated about their Genetic Test Results | Juliann M. | Savatt |
| ELS 177 | A Family Dilemma: Ethical Considerations While Coordinating Familial Testing for an Inherited Telomere Biology Disorder | Lindsey | Schmidt |
| ELS 178 | Genetic Counseling Students and Recent Graduates’ Opinions about Abortion | Courtney | Schuiteman |
| ELS 179 | Knowledge and Attitudes About Privacy and Secondary Data Use Among African Americans Consumers Using Direct-to-Consumer Genetic Testing | Emily | Ziegler |
| Day 2 | |||
| GGT 180 | Post Mortem Genetic Testing in Sudden Unexpected Death in Epilepsy [SUDEP]: A Pilot Study | Yu | An |
| GGT 181 | Clinically Actionable Findings Derived from Predictive Genomic Testing Offered in a Medical Practice Setting | Jennifer | Anderson, MS, LCGC |
| GGT 182 | Cost-Effectiveness Analysis of Newborn Screening for Spinal Muscular Atrophy in the United States | Ramesh | Arjunji |
| GGT 183 | Mitochondrial Replacement Therapy: Genetic Counselors’ Experiences, Knowledge and Opinions | Anjali | Aryamvally |
| GGT 184 | The Role of Genetic Counseling Self-Efficacy in Variant Interpretation Discrepancies | Brenna | Bentley |
| GGT 185 | Preimplantation Genetic Testing: Indications for use and characteristics of users over 8 years at a single institution | Megan | Bunnell, MD, MS GCG |
| GGT 186 | Improving Exome Sequencing Diagnostic Rate by Investigation of Unsolved Cases | Caitlin | Chisholm |
| GGT 187 | Tools for Genetic Counseling Sessions with Direct to Consumer Genetic Testing Clients | Allison | Costa, BS, BA |
| GGT 188 | Adopted Individuals’ Interest in Elective Genomic Testing | Jessica | Edgar |
| GGT 189 | Making somatic less enigmatic: A survey of genetic counselors working in the somatic arena | Dana | Farengo-Clark |
| GGT 190 | Utility of Adding Phenotypic Criteria Refinement to ACMG Guidelines | Lauren | Frank |
| GGT 191 | The Potential Incorporation of Pharmacogenetic Testing into the Genetic Counseling Practice | Zoey | Freedman |
| GGT 192 | A method to improve genetic diagnostic yield among patients suspected to have primary immunodeficiency | Kim | Gall |
| GGT 193 | Genetic Counselors’ Decision-Making in the Utilization of Polygenic Risk Scores in Breast Cancer Clinical Care | Rachel | Gosselin |
| GGT 194 | Participant Outcomes Following Return of Unanticipated Medically Actionable Findings | Melissa | Heller |
| GGT 195 | Genome Sequencing and the Challenges of the Rare Diagnosis in the NICU Setting | Laura | Hendon |
| GGT 196 | The Use of Functional Study in Investigating Variants of Uncertain Significance | Jada | Jackson |
| GGT 197 | An evidence-based evaluation of guidelines criteria for condition inclusion on ECS panels: identifying a guidelines-compliant panel | Katie | Johansen Taber |
| GGT 198 | Performance of a targeted cell-free DNA prenatal test for 22q11.2 deletions in a large clinical cohort | Katheryn | Jones |
| GGT 199 | Experiences and Preferences of the Amish and Mennonite Regarding Genetic Testing | Torey | Jordan |
| GGT 200 | Correlation of Reported Family History and Identified Genomic Results in a State-Funded Population Screening Research Initiative | Whitley V. | Kelley |
| GGT 201 | Two novel cases of biallelic variants in TARS2 presenting with hypotonia, psychomotor delay, cerebellar atrophy and microcephaly; Further evidence towards classification for a mitochondrial disease gene | Megan | Landsverk |
| GGT 202 | Parental Impressions of Genetic Services for Individuals with Treacher Collins Syndrome | Paige | Ledford |
| GGT 203 | Assessing Patient Attitudes Toward Pharmacogenetic Testing | Grace | Lee |
| GGT 204 | Patient satisfaction with consumer-initiated pharmacogenetic testing and post-test telehealth genetic counseling. | Jacquelyn | Magner |
| GGT 205 | Provider Thoughts and Opinions Towards Expanded Carrier Screening | Derek | Mann |
| GGT 206 | Parental testing plays a significant role in clarification of uncertain genetic test results in the pediatric setting. | Kati | Mason, MS, CGC |
| GGT 207 | Evaluating the Feasibility and Impact of Actively Requesting Clinical History at a Specialty Genetics Reference Laboratory | Jamie | McCreery |
| GGT 208 | Genetic Counselors' Experiences and Current Practices Utilizing Clinically Available Breast Cancer Polygenic Risk Scores | Molly | McGuinness |
| GGT 209 | Novel Screening for Advanced Paternal Age using Non-invasive Prenatal Testing for Single-Gene Disorders | Pooja | Mohan |
| GGT 210 | Early Insights on Patient Engagement in a Bi-directional Network Informs Future Development of an Interactive Genome Management Platform | Ana | Morales |
| GGT 211 | The Role of Allele-Specific RNA Analysis in Hereditary Cancer Variant Classification | Erin | Mundt |
| GGT 212 | Carrier Screening for X-linked Conditions is Common Practice | Dana | Neitzel |
| GGT 213 | Elucidating the phenotypic variability associated with the polyT tract in CFTR | Keith | Nykamp |
| GGT 214 | Collaborative approach to clinical correlation and variant interpretation provides diagnosis for 2 brothers with KDM6A variant | Emily H. | Palen |
| GGT 215 | Clinical outcomes of rare chromosomal abnormalities detected by a whole-genome non-invasive prenatal screening assay | Sarah | Paolucci |
| GGT 216 | Creating a source of truth: The Sanford experience with centralizing genomic information in the medical record. | Erin | Royer |
| GGT 217 | Prenatal theoretical diagnostic yield of a rapid, targeted genetic panel designed for critically ill pediatric patients. | Danuta | Stachiw-Hietpas |
| GGT 218 | Molecular Testing for ADPKD in Pediatric and Adult Cohorts Reveals Increased Incidence of PKD1 Truncating Variants in the Pediatric Population | Laura | Sulmonte |
| GGT 219 | Genetic Characterization of Shwachman Diamond Syndrome | Ashley S. | Thompson |
| GGT 220 | Unblurring the ultrasound lines: 45% of infants with prenatal findings receive a reportable result on diagnostic exome sequencing | Meghan | Towne |
| GGT 221 | Clinical outcomes of preimplantation genetic testing for hereditary cancer predisposition syndromes: A systematic review | Natalie | Vriesen |
| GGT 222 | Detecting Novel SNVs and Indels in Alpha Thalassemia Carriers | J. Sherry | Wang |
| PED 223 | Long-Term Outcomes of Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) | Faria | Ahmed |
| PED 224 | Supplemental Newborn and Pediatric Screening: Insight into Consumers and Results | Stephanie | Ashley, MGC, CGC |
| PED 225 | A recurrent DMD deletion in boys referred to genetics for cognitive and neurobehavioral disorders | Miriam | Bunch |
| PED 226 | Exploring Mothers' Experiences with their Child's Diagnosis of Hypermobile Ehlers Danlos Syndrome | Lauren | DeMeyer |
| PED 227 | Development of a Children's Book on Infertility and Family Planning for Girls with Turner Syndrome | Aimee | Durrett, MS, GC |
| PED 228 | Parental Perceptions of Genetic Testing for Hearing Loss: Value and Impact | Briana | Feirstein |
| PED 229 | Step by step: Diagnosis of rare mesoaxial synostotic syndactyly with phalangeal reduction following cascade testing in the pediatric genetics clinic | Leslie | Granger |
| PED 230 | The Spectrum of Features in Males and Females with Mosaic 45,X +Y | Lindsey | Guzewicz |
| PED 231 | The Economics of Genetic Disease in a Level IV NICU: Diagnostic Approaches and Cost of Care | Leanne | Hagen |
| PED 232 | The Parental Perspective of Waiting for Pediatric Clinical Whole Exome Sequencing Results | Stephanie | Lucia |
| PED 233 | EXPERIENCES WITH AND KNOWLEDGE OF GENETICS IN FAMILIES AFFECTED BY CONGENITAL ADRENAL HYPERPLASIA: THE PARENT PERSPECTIVE | Christine | Macica |
| PED 234 | Ultra-rare Diagnoses Highlighting the Importance of Variant of Uncertain Significance Interpretation | Kari | Magnussen |
| PED 235 | Epistaxis and Telangiectasias: Hereditary Hemorrhagic Telangiectasia (HHT) compared to the General Population | Jamie | McDonald |
| PED 236 | Open Operculum in Association with 22q11.2 Deletion Syndrome: An Underreported Diagnostic Biomarker Possibly Linked with Delay in Emergence of Language | Jessica | Merberg, MS |
| PED 237 | Continuing a Search for a Diagnosis: Perspectives from Parents of Children with Undiagnosed Diseases | Ilana | Miller |
| PED 238 | Anxiety, depression, and uncertainty impact quality of life in parents of children with a positive X-linked adrenoleukodystrophy newborn screen | Kayla | Muirhead |
| PED 239 | An Unusual Presentation of Rubinstein-Taybi Syndrome: Genetic Counseling Challenges | Megan | Parker Fonville, MS, CGC |
| PED 240 | Pitt-Hopkins syndrome: consider in the differential diagnosis in pediatric patients with global developmental delays | Chana | Ratner |
| PED 241 | Expanding the Phenotype of Xia Gibbs Syndrome: A Case Report on Patient with a Novel ADHC1 Variant | Kelly | Roche |
| PED 242 | Pediatric genetic counseling: a practice analysis and perspectives from pediatric genetic counselors - a consortium study | Alyssa | Sherwood |
| PED 243 | Not alone anymore: parent and sibling experiences finding support with an ultra-rare diagnosis | Kaitlin C. | Smith |
| PED 244 | Quality of Life of Children with Spinal Muscular Atrophy: Parents' Perspectives in Light of New Treatments | Analyssa | Tallas |
| PED 245 | Novel Cranial Nerve VI Hypoplasia causing lateral rectus palsy with pathogenic variant in PPP1CB | Kerry M | White, MS, LCGC |
| PED 246 | Assessing Interest in Genetic Counseling for Patients with Immune Deficiencies | Victoria | Willingham |
| PRE 247 | Compound heterozygote for Tay Sachs and Sandhoff disease: implications for Tay Sachs carrier testing by enzyme analysis | Alexandra | Barbarese |
| PRE 248 | Factors that Impact Uptake of Carrier Screening in Males | Wendi | Betting |
| PRE 249 | Exploring Factors that Influence Reproductive Decision-Making in Duchenne Muscular Dystrophy Carriers | Caroline | Bong |
| PRE 250 | Parental Questions About Sex Chromosome Aneuploidies Regarding Sex, Gender, and Sexual Orientation in a Prenatal Setting | Sarah | Burzynski, MS |
| PRE 251 | The Impact of Genetic Counseling on Patient Uptake and Satisfaction of Preimplantation Genetic Testing | Alexis | Coates |
| PRE 252 | Enhancement of spinal muscular atrophy carrier screening with unique variants: to include or not to include? | Linda | Cheng |
| PRE 253 | Mosaic Trisomy 13 Detected by Cell-Free DNA: Important Counseling Considerations for a Variable Phenotype | Nicole | Choy |
| PRE 254 | Utilization of Expanded Carrier Screening by Reproductive Genetic Counselors | Emily | Collins |
| PRE 255 | The Impact of Abortion Laws on Prenatal Genetic Counseling: A Comparison Between States | Casey | Crawford, MS |
| PRE 256 | Non-Invasive Prenatal Screening Results Suggestive of Maternal Malignancy: The Genetic Counselor's Experience | Taylor | Durant |
| PRE 257 | Using invasive testing rates and pregnancy outcomes to guide genetic counseling for patients who receive a failed cell-free fetal DNA screening. | Jennifer | Dykeman |
| PRE 258 | Diagnostic testing trends after genome-wide cell-free DNA prenatal screening results | Kimberly | Fanelli |
| PRE 259 | Physician Opinions on Mosaicism in Preimplantation Genetic Screening and Genetic Counseling | Irene | Ford |
| PRE 260 | Knowledge, perceptions, and current trends in carrier screening among Orthodox Jewish young adults | Yoheved | Gerstein |
| PRE 261 | Challenges in genetic counseling for renal anomalies | Ping | Gong |
| PRE 262 | Exploring the benefits, limitations, and impacts of reproductive carrier screening and telehealth-based genetic counseling for individuals found to have an increased reproductive risk | Melanie | Hardy |
| PRE 263 | Experiences of prenatal genetic counselors with abortion regulations in Ohio | Anne | Heuerman |
| PRE 264 | Family Communication of Genetic Results Found on Expanded Carrier Screening | Haley | Hill, MS |
| PRE 265 | Cell free DNA screening for copy number variants secures a diagnosis of Wolf-Hirschhorn syndrome in a pregnancy with suspected anomalies | Natalie | Jacob |
| PRE 266 | Female and Male Perspectives on the Involvement of Male Partners in Expanded Carrier Screening | Sarah | Jurgensmeyer |
| PRE 267 | A Familial Xq Deletion/Duplication Ascertained Incidentally via Sequencing-Based Expanded Carrier Screening | Olga | Latosh |
| PRE 268 | Prenatal Diagnosis of Swyer Syndrome due to Discordance Between cfDNA and Fetal Ultrasound | Enrique | Lopez |
| PRE 269 | Reporting and Transfer of Mosaic Embryos: Experiences and Attitudes of Genetic Counselors | Casey | Marks |
| PRE 270 | Prenatal ascertainment of Bardet Biedl syndrome that was missed by expanded carrier screening | Erin | McGraw |
| PRE 271 | Pregnancy, Genetic Counseling and Cystic Fibrosis: Exploring the experiences and discussions between females with CF and their health care providers. | Morgan | McManus |
| PRE 272 | Assessing Social Media for Themes of Trisomy 18 and 13 | Falecia | Metcalf |
| PRE 273 | Omphalocele and monosomy X: expanding the phenotype of 45,X through first trimester ultrasound | Kristen | Miller |
| PRE 274 | EXPERIENCE WITH PREIMPLANTATION GENETIC TESTING FOR CONDITIONS THAT ARE FOUND TO BE DE NOVO IN CHILD | Rachel | Mnushkin |
| PRE 275 | Expanded Carrier Screening allowed Prenatal Diagnosis of Congenital Finnish Nephrosis without Diagnostic Testing | Alexis | Morgan |
| PRE 276 | Prenatal diagnosis of mosaic 45,X/46,X,idic(Y) after discordant findings from cell free DNA and prenatal ultrasound: A case series | Lauren | Petrarca |
| PRE 277 | The Emotional Impact of Restrictive Abortion Laws on Prenatal Genetic Counselors | Elizabeth | Pollard |
| PRE 278 | Genetic counseling on road to a complex familial diagnosis: A lethal ciliopathy. | Nivedita | Rajakumar |
| PRE 279 | Genetic counselors’ experiences with transgender individuals in prenatal and preconception settings | Maggie | Ruderman |
| PRE 280 | Diagnostic Testing Uptake Rates in Fragile X Premutation Carriers and Couples At Risk for an Autosomal Recessive Condition in Their Offspring | Kendall | Snyder |
| PRE 281 | “Desbu-what?”: Rare diagnosis highlights limitations of ultrasound parameters suggestive of lethal skeletal dysplasia | Samantha | Stover |
| PRE 282 | Prenatal Genetic Testing Decisions After In Vitro Fertilization with Preimplantation Genetic Testing | Marina | Sumarroca |
| PRE 283 | Patient Knowledge of, Attitudes Toward, and Perceived Utility of Carrier Screening in an Obstetric Setting | Rachel | Thomas |
| PRE 284 | Noninvasive Prenatal Screening For Copy Number Variants: Opinions and Current Use By Prenatal Genetic Counselors | Kara | Vitalone |
| PRE 285 | Biallelic variants in MYMK as a novel cause of recurrent cystic hygroma and early fetal hydrops in two consecutive pregnancies: Phenotypic expansion of Carey-Fineman-Ziter syndrome | Lauren | Westerfield |
| PRE 286 | Revisiting the Essential Informational Needs of Parents Receiving a Diagnosis of Down Syndrome | Margaret | Wilkes |
| PRE 287 | NGS Panel Testing in the Prenatal Diagnosis of RASopathies in Fetuses with Abnormal Ultrasound Findings | Bradley | Williams |
| PI 288 | Tracking and Management of Variants of Uncertain Significance in Clinics Over Time | Elise | Bergin |
| PI 289 | Techniques to Facilitate Communication Among Racially And Ethnically Isolated Genetic Professionals | Austin | Bland |
| PI 290 | Career Ladder Development: Insights and Experiences from Both Clinical and Industry Genetic Counselors | Hayley | Bottino |
| PI 291 | A National Sampling of Characteristics of a Genetic Counselor Career Ladder | Hayley | Bottino |
| PI 292 | Exploring the Integration of Adverse Childhood Experiences in Genetic Counseling Practice | Hannah | Brodner |
| PI 293 | GCs become established in a new position in 4 months, as indicated by decreases in documentation time | Colleen | Caleshu |
| PI 294 | Peer-Reviewed Outcomes and Perceptions of Genetic Counseling Student Research | Caitlin | Clark-Wiest |
| PI 295 | Exploring Genetic Counselors’ Perceptions and Attitudes Towards Preimplantation Genetic Testing for Aneuploidy (PGT-A) | Danika | Coulson |
| PI 296 | An Academic RVU for Genetic Counselors: Development of a Tool to Measure Productivity | Sandra | Darilek |
| PI 297 | Misinterpretation of Genetic Test Results by Healthcare Providers | Katherine | Donohue |
| PI 298 | An Exploration of Genetic Counselors’ Use and Application of Family Health History Tools | Pankti | Doshi |
| PI 299 | Bridging the Gap between Genetic Counselors and Special Education: A Survey on Genetic Counselors' Knowledge and Attitudes | Rosetta | Dowling |
| PI 300 | Improving Access to Potential Genetic Counseling Students through High School Counselors | Summer | Duffy |
| PI 301 | Genetic Counseling Job Search: Facilitators and Barriers | Sierra | Dyer |
| PI 302 | Does Experience Matter? An Examination of the Factors Influencing Application and Acceptance of Jobs by Genetic Counselors | Sierra | Dyer |
| PI 303 | Laboratory Genetic Counselors’ Motivations for Choosing this Practice Specialty: A Qualitative Investigation | Maribeth | Golm |
| PI 304 | Investigating the Factors That Affect Providers’ Discussion of Pre-Implantation Genetic Testing for Adult-Onset Hereditary Cancer Syndromes in Gene Positive Patients | Ashley | Kennes |
| PI 305 | The “Floating GCA”: Introducing a Multidisciplinary Genetic Counseling Assistant in an Academic Hospital | Courtney E. | Leonard |
| PI 306 | : Involvement of Genetic Counselors at State-Level Association in Pennsylvania | Claire | Nelson |
| PI 307 | Exploring the experience of reapplying for admission to genetic counseling programs after initial rejection | Gabrielle | Pomorski |
| PI 308 | INTRAPERSONAL AND DEMOGRAPHIC PREDICTORS OF COMPASSION FATIGUE IN GENETIC COUNSELORS: A MULTIPLE VARIABLE INVESTIGATION | Jimena F | Prado Hernandez |
| PI 309 | Defining the Roles of Laboratory Genetic Counseling Assistants and Important Factors in the Genetic Counselor – Genetic Counseling Assistant (GC-GCA) Relationship | Jordyn | Prell |
| PI 310 | How Genetic Counselors Remain Informed of Practice Guidelines. | Samantha | Sandlow |
| PI 311 | Geographical Analysis of the Distribution of Certified Genetic Counselors in the United States | Karina | Skov |
| PI 312 | THE CAREER ARC OF GENETIC COUNSELORS AND A CHANGING PROFESSIONAL LANDSCAPE | Wanchun | Smires |
| PI 313 | Outcomes of a Genetic Counseling Assistant Mentorship Program | Elise | Watson |
| PI 314 | Perceived Value of Genetic Counseling for Consumer-Initiated Genetic Testing | Nori | Williams, CGC |
| PI 315 | Life Outside Clinic: The Lived Experiences and Family Planning Decisions of Genetic Counselors Working with Pediatric Patients | Kristen | Wong |
| PI 316 | Diverse Career Considerations of Potential Genetic Counseling Applicants | Rachel | Wyatt |
| NEU 317 | Presenting Features and the Availability of Parental Testing Strongly Influence Diagnostic Rates of Multi-Gene Panels for Brain Malformation Disorders | Sohnee | Ahmed |
| NEU 318 | Characterization of Depressive Symptoms in Individuals with Reduced Penetrance Huntington’s Disease Allele Expansions using Enroll-HD | Christina | Dailey |
| NEU 319 | “IT TAKES AWAY WHAT MADE A PERSON THAT PERSON”: RECONSTRUCTING IDENTITY IN RESPONSE TO GENETIC RISK OF BEHAVIORAL VARIANT FRONTOTEMPORAL DEMENTIA | Laynie | Dratch |
| NEU 320 | Nuclear localization of ATXN1 in extra-cerebellar SCA1 pathology | Hillary | Handler |
| NEU 321 | Perceptions of Social Rejection and Fear in Individuals with Mosaic Down Syndrome | Quinn | Hurshman |
| NEU 322 | The ALS Genetic Access Program: Paving the Way for Genetic Testing, Counseling and Therapy for ALS | Jennifer | Roggenbuck |
| NEU 323 | An Investigation into the reasons behind quality of life perception in individuals with HNPP as compared to individuals with CMT1A | Caitlin | Walsh |
| PH 324 | Insurance Coverage Impacts the Clinical Use of Prenatal Chromosomal Aneuploidy Screening: Implications for Health Equity | Megan | Benoy |
| PH 325 | Estimating the need for and utilization of allogeneic hematopoietic cell transplantation (alloHCT) to treat severe combined immunodeficiency (SCID) | Anna | DeSalvo, MS, CGC |
| PH 326 | Patient Navigators vs. Electronic Medical Record Messaging: Genetic counseling appointment completion in an underserved population | Amber | Gemmell |
| PH 327 | Assessment of Cancer Risk Understanding and Motivations of Individuals Receiving Negative Screening Results in the Healthy Oregon Project | Emily | Guilbert |
| PH 328 | Primary Care for Rare Disease Patients: Exploring services received, healthcare providers involved, and patient satisfaction | Catherine | Mayo |
| PH 329 | Tower of Babel: A Qualitative Cross-Site Comparison of Provider Terminology when Discussing Universal Lynch Syndrome Screening | Zachary | Salvati |
| RI 330 | Attitudes About Data Sharing in Parent and Adolescent Participants in a Pediatric Genomic Research Repository | Courtney | Berrios |
| RI 331 | What is ‘Usual Care’ in Genetic Counseling Research? Evidence from CSER Consortium Studies | Barbara | Biesecker |
| RI 332 | Biobank set-up and execution: A retrospective effort analysis | Carrie | Blout |
| RI 333 | Developing a framework for performing genotype-phenotype analyses using a real-world data platform | Kristina | Cotter |
| RI 334 | The Million Veteran Program - Return Of Actionable Results (MVP-ROAR) Study: Design and Pilot Results | Morgan | Danowski |
| RI 335 | Variant reclassifications at the intersection of research and clinical care | Emma | Perez |
| RI 336 | Spatial and nonspatial barriers to Undiagnosed Diseases Network acceptance: Implications for accessing research | Gianna | Petrelli |
| RI 337 | Declining medically actionable genetic results: Why Mass General Brigham Biobank participants opt out of clinical result confirmation | Janelle | Shea, BS, BA |
| UM 338 | Work Smarter, Not Harder: Use of a Dynamic Database to Streamline Test Utilization Management | Sarah | Arneson |
| UM 339 | Implementation and Cost Savings of Optional Pre-authorization at a Large Pediatric Institution | Kathleen | Collins Ruff |
| UM 340 | Implementation of genetic carrier screening in the OB population: healthcare cost impact and recommendation adherence | Aranza | Gonzalez Cendejas |
| UM 341 | Current hereditary cancer reflex testing practices for Ashkenazi Jewish individuals, a large commercial laboratory’s experience | Mary | Hricik |
| UM 342 | Assessing the Impact of a Genetic Counseling Assistant at a Hematology Reference Laboratory | Stefanie | Dugan, MS, CGC |
| UM 343 | Genetic Counselors’ Involvement and Perceived Impact in the IEP and 504 School Accommodations Process | Kaitlin | Oconnell |
| UM 344 | Assessing The Current Landscape of National Payer Policy Regarding Genetic Counseling Services and Billing Practices | Eric | Tricou |
| UM 345 | Laboratory Genetic Counseling Assistant Adds Value to a Genetic Test Stewardship Program | Claire | Wittowski |
| CAN 346 | A Variant in the PMS2 Gene versus PMSCL pseudogene in a Patient with Prostate Cancer: Implications for Patient Counseling and Additional Testing | Amanda | Schott |